A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8175n54



Internal ID22776070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4032349..4124049hg38UCSC Ensembl
chr3:4074033..4165733hg19UCSC Ensembl
chr3:4049033..4140733hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3891701
hg1991701
hg1891701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589419, nsv589411
SamplesHGDP00993, HGDP01333
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8175n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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